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protect the blood-brain barrier against oxidative stress by activating the Nrf2 signaling to regulate inflammation-related genes such as GSH ( 25 ). H/R-induced injury was also implicated in hepatocytes by promoting apoptosis and oxidative stress through
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disrupters, molecular mechanisms and detection methods . Therapie 2007 62 369 – 386 . ( https://doi.org/10.2515/therapie:2007062 ) 11 Bhardwaj JK Saraf P . Granulosa cell apoptosis by impairing antioxidant defense system and cellular integrity
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signaling including IRS1, AKT and GSK-3β were hypophosphorylated in LKO hepatocytes, which subsequently blunt glucose uptake ( 21 ). SGK1 also exerts dramatic liver protection effect. Existing researches revealed that SGK1 alleviates hepatocyte apoptosis via
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β-cells. The permanent increase in intracellular calcium, however, increases the apoptosis and decreases pancreatic β-cell mass during adulthood, leading these transgenic mice to a switch to a hyperglycemic phenotype later in life ( 28 ). This
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most important physiologic regulators of calcium and phosphate metabolism, together with the kidney. In bone, low extracellular phosphate concentration is crucial for apoptosis of mature chondrocytes in the growth plate and the cascade of events leading
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skeletal muscle protein synthesis and breakdown, as well as apoptosis ( 15 ). Inhibition of Akt phosphorylation was also responsible for simvastatin-induced mitochondrial dysfunction in mouse C2C12 muscle cells ( 16 ). Potential mechanisms for simvastatin
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Shanghai National Clinical Research Center for Metabolic Diseases, Key Laboratory for Endocrine and Metabolic Diseases of the National Health Commission of the PR China, Shanghai National Center for Translational Medicine, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China
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mRNA with target prediction of differentially expressed lncRNAs, and NRCAM and JUNB were identified. Previous reports showed that NRCAM can activate ERK and AKT pathway to inhibit cell apoptosis and promote cell proliferation ( 38 , 39 , 40
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factor GATA-6, cell proliferation, apoptosis, and apoptosis-related proteins Bcl-2 and Bax in human fetal testis . Journal of Clinical Endocrinology and Metabolism 2003 88 1858 – 1865 . ( doi:10.1210/jc.2002-021647 ) 10.1210/jc.2002-021647 38
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). Furthermore, functional studies in breast cancer highlighted an important role of SDPR in apoptosis promotion ( 36 ) and in the suppression of the epithelial–mesenchymal transition ( 54 ). Lastly, SLC26A4 encodes for pendrin, a chloride–iodide transporter
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